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Genetaq | Researchclopedia

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Genetaq

Málaga del Fresnofacility

12

Works

365

Citations

14

h-index

Top Research Topics

Mitochondrial Function and Pathology Metabolism and Genetic Disorders Polyomavirus and related diseases

Top Researchers

J.A. Siles University of Córdoba

98 works3,819 citationsh-index: 36

Recent Research

New mutation of the ceruloplasmin gene in the case of a neurologically asymptomatic patient with microcytic anaemia, obesity and supposed Wilson’s disease

Mária Ondrejkovičová,Sylvia Dražilová,et al.

202011 citations

ATP Synthase and ATPases Research

Full-Duplex Wireless Communications

Influenza Virus Research Studies

Sarcoma Diagnosis and Treatment

Diabetes Treatment and Management

Iron Metabolism and Disorders

Pneumonia and Respiratory Infections

Pancreatic function and diabetes

Amyotrophic Lateral Sclerosis Research

Carlos Sánchez‐Linares Universidad de Málaga

71 works841 citationsh-index: 18

José Miguel Lezana Rosales Hospital Universitario 12 De Octubre

23 works353 citationsh-index: 10

Carmen Palma Milla Hospital Universitario 12 De Octubre

37 works245 citationsh-index: 10

Juan López Siles Genetaq

14 works209 citationsh-index: 7

Pilar Carrasco Salas Hospital Juan Ramón Jiménez

26 works88 citationsh-index: 5

The solitary median maxillary central incisor (SMMCI) syndrome: Associations, prenatal diagnosis, and outcomes

R. García Rodríguez,Loida García Cruz,et al.

201917 citations

Neurofibromatosis type I: mutation spectrum of <i>NF1</i> in spanish patients

Carmen Palma Milla,José Miguel Lezana Rosales,et al.

201816 citations

Leber hereditary optic neuropathy: Usefulness of next generation sequencing to study mitochondrial mutations on apparent homoplasmy

Pilar Carrasco Salas,Carmen Palma Milla,et al.

20168 citations

Neuropatía óptica de Leber: utilidad de la secuenciación masiva en el estudio de mutaciones mitocondriales en aparente homoplasmia

Pilar Carrasco Salas,Carmen Palma Milla,et al.

20154 citations

Hyperinsulinemic hypoglycemia in a patient with an intragenic NSD1 mutation

Pilar Carrasco Salas,Carmen Palma Milla,et al.

20157 citations